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在缺乏30S核糖体亚基的大肠杆菌中乳糖操纵子mRNA的合成与降解

Synthesis and degradation of lac mRNA in E. coli depleted of 30S ribosomal subunits.

作者信息

Har-El R, Silberstein A, Kuhn J, Tal M

出版信息

Mol Gen Genet. 1979 Jun 7;173(2):135-44. doi: 10.1007/BF00330303.

Abstract

Escherichia coli was depleted of active ribosomes by a thermal shock at 47 degrees C which quantitatively destroyed the 30S ribosomal subunits. During recovery, RNA is synthesized while protein synthesis resumes only after about 90 minutes. It is shown that lac mRNA is synthesized in the complete absence of ribosomal activity and hence RNA synthesis is not coupled to protein synthesis. Transcription time and average transcript length were slightly less than in untreated cells. lac mRNA was degraded much more slowly in bacteria depleted of ribosomes. In E. coli W both functional half life (T 1/2 = 28 min vs. 2.25 in untreated cells) and chemical stability. The analysis of rna and pnp mutants showed that polynucleotide phosphorylase is involved in lac mRNA degradation in heat treated cells but that RNase I is not. The functional T 1/2 was increased in pnp mutants and was 95 min during the recovery period. The rate of chemical decay is so slow that the half-life cannot be accurately determined.

摘要

通过在47摄氏度的热休克处理,使大肠杆菌中的活性核糖体减少,这种处理定量地破坏了30S核糖体亚基。在恢复过程中,RNA进行合成,而蛋白质合成仅在约90分钟后才恢复。结果表明,lac mRNA在完全没有核糖体活性的情况下合成,因此RNA合成与蛋白质合成不偶联。转录时间和平均转录本长度略小于未处理的细胞。在核糖体减少的细菌中,lac mRNA的降解要慢得多。在大肠杆菌W中,功能性半衰期(T1/2 = 28分钟,未处理细胞中为2.25分钟)和化学稳定性均如此。对rna和pnp突变体的分析表明,多核苷酸磷酸化酶参与热处理细胞中lac mRNA的降解,但核糖核酸酶I不参与。在pnp突变体中,功能性T1/2增加,在恢复期为95分钟。化学衰变速率非常缓慢,以至于半衰期无法准确测定。

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